Active ingredient

Miconazole nitrate 2%

Purpose

antifungal

Use (Athlete's Foot)

for the cure of most athlete's foot

Warnings

For external use only

Do not use

on children under 2 years of age unless directed by a doctor.

Avoid contact with the eyes.

Stop use and ask a doctor if (Athlete's Foot)

irritation occurs or there is no improvement within 4 weeks.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions (Athlete's Foot)

Clean the affected area and dry thoroughly.
Apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor.
Supervise children in the use of this product.
Pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.
Use daily for 4 weeks.
If condition persists longer, consult a doctor.
This product is not effective on the scalp or nails.

Other information

Product settles during shipment. Package contains full net weight.

Inactive ingredients

acrylamide/sodium acrylate copolymer, aldioxa, chloroxylenol, fragrance, imidurea, microporous cellulose, talc. Contains no starch.

Questions?

call 1-888-438-7426. Side effects should be reported to this number.

Manufactured for: Stiefel Laboratories, Inc. Research Triangle Park, NC 27709

www.zeasorb.com

IRONMAN® is a registered trademark of World Triathlon Corporation used herein by permission.

ZEASORB is a registered trademark of Stiefel Laboratories, Inc.

Additional barcode labeling by:
Physicians Total Care, inc.
Tulsa, Oklahoma 74146

Principal Display Panel

NDC 54868-5876-0

Zeasorb Antifungal Treatment Athlete's foot 2.5 oz (71 g) front label

Zeasorb®

ANTIFUNGAL TREATMENT

Miconazole Nitrate 2%

Super Absorbent Powder

cures most

athlete's foot

Relieves:

Itching
Burning
Scaling

Official Partner IRONMAN®

Net Wt. 2.5 Oz (71g)

ZEASORB AF
miconazole nitrate powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54868-5876(NDC:0145-1506)
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M)	MICONAZOLE NITRATE	20.6 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
ACRYLAMIDE (UNII: 20R035KLCI)
ALDIOXA (UNII: 8T66I31YNK)
CHLOROXYLENOL (UNII: 0F32U78V2Q)
IMIDUREA (UNII: M629807ATL)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
TALC (UNII: 7SEV7J4R1U)

Product Characteristics
Color	WHITE (white to off-white)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:54868-5876-0	71 g in 1 BOTTLE

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333C	03/31/2008

Labeler - Physicians Total Care, Inc. (194123980)

Name	Address	ID/FEI	Business Operations
Establishment
Physicians Total Care, Inc.		194123980	relabel

Drug Facts